K-number	K202880
Device name	J-Plasma Precise FLEX Handpiece
Applicant	Apyx Medical Corporation (Formerly Bovie Medical Corporation
Product code	GEI
Device class	Class II
Decision date	Jan 4, 2021
Decision	Substantially Equivalent
Regulation	—

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Source

View the full FDA submission: accessdata.fda.gov

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J-Plasma Precise FLEX Handpiece

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